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Supervisor, Manufacturing

Job in Waltham, Middlesex County, Massachusetts, 02254, USA
Listing for: ElevateBio
Per diem position
Listed on 2026-06-10
Job specializations:
  • Manufacturing / Production
    Manufacturing Engineer, Operations Engineer, Pharmaceutical Manufacturing
Salary/Wage Range or Industry Benchmark: 50 - 69 USD Hourly USD 50.00 69.00 HOUR
Job Description & How to Apply Below

Elevate Bio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently.

The Role:

Elevate Bio is looking for a dynamic individual to join and contribute to building the manufacturing operations team at our Base Camp facility. The incumbent will ultimately perform routine cGMP manufacture of multiple cell and gene therapy types/products at our state-of-the-art Base Camp facility such as CAR-Ts, iPSCs, TILs, and mRNA. The individual should be a motivated self-starter eager to contribute to supporting a manufacturing organization unparalleled in its capabilities and expertise, have a willingness and aptitude for adoption of new technology, an ability to build relationships and work effectively in a cross‑functional team, and commitment to the highest safety and quality standards.

Here’s

What You’ll Do:
  • Lead right-first-time cGMP manufacturing of cell and gene therapy products including but not limited to aseptic processing, cell isolation, selection, culturing, expansion, harvest, cryopreservation and final product visual inspection.
  • Lead manufacturing activities including but not limited to authoring SOPs, batch records, reports, risk assessments, material ordering/management.
  • Provide constructive input on teams for the selection and set-up of equipment, process and material flows, etc.
  • Create and maintain training materials and curricula that support continuous improvement in the cGMP manufacture of cell therapy products.
  • Work effectively with cross functional teams comprised of process development, facilities & engineering, MSAT, quality control and quality assurance to ensure right-first-time technology transfer.
  • Work with Quality Assurance and MSAT to proactively resolve issues such as deviations, CAPAs, Change Controls.
  • Commitment to the highest safety and quality standards in service of our colleagues and patients.
  • Generate and manage batch records, run reports, batch data, etc. for manufacturing and scale-up activities.
  • Proactively identify opportunities for improvements in areas such as safety, quality, delivery and cost.
  • Be integral in providing hands-on technical, organizational, and leadership expertise to the manufacturing department including but not limited to equipment selection, SOPs, batch records, reports, risk assessments, material ordering/management.
  • Ensure the safety of assigned areas and work practices in accordance with EHS program. Ensure JHA (Job Hazard Analysis) are reviewed regularly, and pre-job briefs are in place prior to execution.
  • Provide daily management oversight for the team and ensure processes are executed with cGMP.
  • Recruit and develop staff, maintain, and report department metrics to drive operational improvement.
  • Balance and prioritize daily production demands to ensure right first-time execution.
Requirements:
  • Bachelor’s degree in biological science(s) field or related engineering with 4-6 years of experience in cGMP biotech manufacturing, preferably cell and gene therapies.
  • 2+ years of experience in people leading and/or project leadership.
  • Experience with some or all of the following: cGMP manufacture and/or process development for CART, TCR, TIL, cellular therapies, and mRNA.
  • Advanced understanding of primary cell culture and experience with equipment including but not limited to BSC, Microscope, LOVO, Clini

    MACS, Incubators, Centrifuges, CRF, and G‑Rex systems.
  • Outstanding communication skills (verbal and written).
  • Excellent computer and word processing skills including Microsoft Excel, PowerPoint, and Word.
  • Demonstrate proficiency in aseptic technique and/or processing.
  • Ability to function in dynamic environment and balance multiple priorities simultaneously.
Work Schedule:
  • Must be available to overtime on weekdays, weekends and holidays as needed.
Physical Requirements:
  • Employee will frequently stand, walk, bend, stretch for extended periods.
  • Routinely carry up to 25 pounds and up to 50 pounds.
  • Routinely…
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